A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962822



Internal ID19208698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:82131085..82159689hg38UCSC Ensembl
Outerchr16:82164690..82193294hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3828605
hg1928605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129383
Supporting Variants
SamplesKWS1
Known GenesMPHOSPH6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962822
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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